Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion-Reference-Cited by-同舟云学术

Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion

Published:2005-02 Issue:3 Volume:128 Page:380-385
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Hewitt Jeff,Ballard Jennifer N. M.,Nelson Tanya N.,Smith Valerie C.,Griffiths Tanya A. M.,Pritchard Sheila,Wu John K.,Wadsworth Louis D.,Casey Brett,MacGillivray Ross T. A.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2004.05296.x/fullpdf

Reference30 articles.

1. The Solution Structure of Human Coagulation Factor VIIa in Its Complex with Tissue Factor Is Similar to Free Factor VIIa: A Study of a Heterodimeric Receptor−Ligand Complex by X-ray and Neutron Scattering and Computational Modeling

2. The Factor Vlla / Tissue Factor Complex

3. The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor

4. Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: A summary of case reports

5. The Factor VII Zymogen Structure Reveals Reregistration of β Strands during Activation

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Factor VII Deficiency, Diagnosis, and Management;Congenital Bleeding Disorders;2023

2. Coagulation Factor VII: Genetic, Molecular, and Clinical Characteristics;Trends in Medical Sciences;2022-06-22

3. Factor VII Deficiency Due to Compound Heterozygosity for the p.Leu13Pro Mutation and a Novel Mutation in the HNF4 Binding Region (−58G>C) in the <i>F7</i> Promoter;The Kurume Medical Journal;2020-09-30

4. Novel IVS7+1G>T mutation of life-threatening congenital factor VII deficiency in neonates;Medicine;2019-10

5. Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes;Haemophilia;2011-11-30